Canonical Allele Identifier: CA2683610083
Gene: ABCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87600877del , CM000669.2:g.87600877del GRCh38
NC_000007.13:g.87230193del , CM000669.1:g.87230193del GRCh37
NC_000007.12:g.87068129del NCBI36
NG_011513.1:g.117372del

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.-129del ENSP00000265724.3:n.-129del
ENST00000622132.5:c.-129del MANE Select ENSP00000478255.1:n.-129del
ENST00000265724.7:c.-129del ENSP00000265724.3:n.-129del
ENST00000416177.1:c.-77-52del ENSP00000399419.1:n.-77-52del
ENST00000476862.1:n.518del
ENST00000543898.5:c.-129del ENSP00000444095.1:n.-129del
ENST00000622132.4:c.-129del ENSP00000478255.1:n.-129del
NM_000927.4:c.-129del NP_000918.2:n.-129del
NM_001348944.1:c.-77-52del NP_001335873.1:n.-77-52del
NM_001348945.1:c.134-52del NP_001335874.1:n.134-52del
NM_001348946.1:c.-129del NP_001335875.1:n.-129del
NM_001348946.2:c.-129del MANE Select NP_001335875.1:n.-129del
NM_000927.5:c.-129del NP_000918.2:n.-129del
NM_001348944.2:c.-77-52del NP_001335873.1:n.-77-52del
NM_001348945.2:c.134-52del NP_001335874.1:n.134-52del